Canonical Allele Identifier: CA449666920

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625047T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657270T>C , CM000668.2:g.31657270T>C	GRCh38
NC_000006.11:g.31625047T>C , CM000668.1:g.31625047T>C	GRCh37
NC_000006.10:g.31733026T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.315T>C (APOM) MANE Select	ENSP00000365081.3:p.Thr105=
ENST00000375916.3:c.315T>C (APOM)	ENSP00000365081.3:p.Thr105=
ENST00000375918.6:c.99T>C (APOM)	ENSP00000365083.2:p.Thr33=
ENST00000375920.8:c.99T>C (APOM)	ENSP00000365085.4:p.Thr33=
NM_001256169.1:c.99T>C (APOM)	NP_001243098.1:p.Thr33=
NM_019101.2:c.315T>C (APOM)	NP_061974.2:p.Thr105=
NR_045828.1:n.350T>C (APOM)
XM_006715150.2:c.219T>C (APOM)	XP_006715213.1:p.Thr73=
XM_011514895.1:c.-14+3051A>G (BAG6)	XP_011513197.1:n.-14+3051A>G
XM_006715150.3:c.219T>C (APOM)	XP_006715213.1:p.Thr73=
XM_017011279.2:c.-14+3051A>G (BAG6)	XP_016866768.1:n.-14+3051A>G
XM_024446545.1:c.-14+494A>G (BAG6)	XP_024302313.1:n.-14+494A>G
NM_019101.3:c.315T>C (APOM) MANE Select	NP_061974.2:p.Thr105=
NM_001256169.2:c.99T>C (APOM)	NP_001243098.1:p.Thr33=
NR_045828.2:n.356T>C (APOM)